Five-year safety evaluation of maraviroc in HIV-1-infected treatment-experienced patients.

J Acquir Immune Defic Syndr

*Weill Cornell Medical College, New York, NY; †University Hospital of Cologne, Cologne, Germany; ‡Pfizer, Inc, Groton, CT; §David Geffen School of Medicine at UCLA, Los Angeles, CA; ‖Chelsea and Westminster Hospital, London, United Kingdom; ¶ViiV Healthcare, Research Triangle Park, NC; #Pfizer, Inc, New York, NY; and **Bristol-Myers Squibb, Wallingford, CT. 1Deceased.

Published: January 2014

Background: Maraviroc is unique among approved antiretroviral drugs in targeting the host-cell chemokine coreceptor type-5 receptor. With its novel mechanism of action, we sought to describe the 5-year safety profile of maraviroc.

Methods: Two large phase 3 studies of maraviroc enrolled HIV-infected treatment-experienced patients and followed them up for 5 or more years. Survival and selected clinical end points were identified and assessed.

Results: A total of 938 enrolled patients received maraviroc-containing regimens. Rates of death and selected clinical events (eg, hepatic failure, malignancy, and myocardial infarction) were low during follow-up.

Conclusions: Maraviroc was generally safe in treatment-experienced participants for >5 years.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3893710PMC
http://dx.doi.org/10.1097/QAI.0b013e3182a7a97aDOI Listing

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